Tumor immune microenvironment analysis of non-small cell lung cancer development through multiplex immunofluorescence.

Non-small cell lung cancer (NSCLC) adenocarcinoma in situ (AIS) minimally invasive adenocarcinoma (MIA) multiplex immunofluorescence technology (mIF technology) tumor immune microenvironment (TIME)

Journal

Translational lung cancer research
ISSN: 2218-6751
Titre abrégé: Transl Lung Cancer Res
Pays: China
ID NLM: 101646875

Informations de publication

Date de publication:
30 Sep 2024
Historique:
received: 29 04 2024
accepted: 29 08 2024
medline: 21 10 2024
pubmed: 21 10 2024
entrez: 21 10 2024
Statut: ppublish

Résumé

Emerging evidence has underscored the crucial role of infiltrating immune cells in the tumor immune microenvironment (TIME) of non-small cell lung cancer (NSCLC) development and progression. With the implementation of screening programs, the incidence of early-stage NSCLC is rising. However, the high risk of recurrence and poor survival rates associated with this disease necessitate a deeper understanding of the TIME and its relationship with driver alterations. The aim of this study was to provide an in-depth analysis of immune changes in early-stage NSCLC, highlighting the significant transitions in immune response during disease progression. Tumor tissues were collected from 105 patients with precancerous lesions or stage I-III NSCLC. Next-generation sequencing (NGS) was used to detect cancer driver alterations. Multiplex immunofluorescence (mIF) was performed to evaluate immune cell density, percentage, and spatial proximity to cancer cells in the TIME. Next Among these patients, 64 had NGS results, including three with adenocarcinoma in situ (AIS), 10 with minimally invasive adenocarcinoma (MIA), and 51 with stage I invasive cancers. Additionally, three patients underwent neoadjuvant immuno-chemotherapy and tumor tissue specimens before and after treatment were obtained. Patients with stage I invasive cancer had significantly higher density (P=0.01) and percentage (P=0.02) of CD8 This study offers an in-depth analysis of immune changes in NSCLC, demonstrating that the transition from AIS/MIA to invasive stage I NSCLC leads to immune activation, while the advancement from stage I to stage III cancer results in immune suppression. These findings contribute to our understanding of the molecular mechanisms underlying early-stage NSCLC progression and pave the way for the identification of potential treatment options.

Sections du résumé

Background UNASSIGNED
Emerging evidence has underscored the crucial role of infiltrating immune cells in the tumor immune microenvironment (TIME) of non-small cell lung cancer (NSCLC) development and progression. With the implementation of screening programs, the incidence of early-stage NSCLC is rising. However, the high risk of recurrence and poor survival rates associated with this disease necessitate a deeper understanding of the TIME and its relationship with driver alterations. The aim of this study was to provide an in-depth analysis of immune changes in early-stage NSCLC, highlighting the significant transitions in immune response during disease progression.
Methods UNASSIGNED
Tumor tissues were collected from 105 patients with precancerous lesions or stage I-III NSCLC. Next-generation sequencing (NGS) was used to detect cancer driver alterations. Multiplex immunofluorescence (mIF) was performed to evaluate immune cell density, percentage, and spatial proximity to cancer cells in the TIME. Next Among these patients, 64 had NGS results, including three with adenocarcinoma in situ (AIS), 10 with minimally invasive adenocarcinoma (MIA), and 51 with stage I invasive cancers. Additionally, three patients underwent neoadjuvant immuno-chemotherapy and tumor tissue specimens before and after treatment were obtained.
Results UNASSIGNED
Patients with stage I invasive cancer had significantly higher density (P=0.01) and percentage (P=0.02) of CD8
Conclusions UNASSIGNED
This study offers an in-depth analysis of immune changes in NSCLC, demonstrating that the transition from AIS/MIA to invasive stage I NSCLC leads to immune activation, while the advancement from stage I to stage III cancer results in immune suppression. These findings contribute to our understanding of the molecular mechanisms underlying early-stage NSCLC progression and pave the way for the identification of potential treatment options.

Identifiants

pubmed: 39430335
doi: 10.21037/tlcr-24-379
pii: tlcr-13-09-2395
pmc: PMC11484713
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2395-2410

Informations de copyright

2024 AME Publishing Company. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://tlcr.amegroups.com/article/view/10.21037/tlcr-24-379/coif). Y.S. serves as an Editor-in-Chief of Translational Lung Cancer Research. D.Z., J.C., B.Z., Junling Zhang, and M.H. are from 3D Medicines Inc. The other authors have no other conflicts of interest to declare.

Auteurs

Jiaping Zhao (J)

Department of Thoracic Surgery, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.

Yu Lu (Y)

Department of Thoracic Surgery, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.

Zhaofeng Wang (Z)

Department of Respiratory Medicine, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

Haiying Wang (H)

Department of Respiratory, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.

Ding Zhang (D)

Medical Affairs, 3D Medicines, Inc., Shanghai, China.

Jinping Cai (J)

Medical Affairs, 3D Medicines, Inc., Shanghai, China.

Bei Zhang (B)

Medical Affairs, 3D Medicines, Inc., Shanghai, China.

Junling Zhang (J)

Medical Affairs, 3D Medicines, Inc., Shanghai, China.

Mengli Huang (M)

Medical Affairs, 3D Medicines, Inc., Shanghai, China.

Andreas Pircher (A)

Department of Haematology and Oncology, Internal Medicine V, Comprehensive Cancer Center Innsbruck (CCCI), Medical University of Innsbruck (MUI), Innsbruck, Austria.

Krishna H Patel (KH)

Institute for Translational Epidemiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Honggang Ke (H)

Department of Thoracic Surgery, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.

Yong Song (Y)

Department of Respiratory Medicine, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.

Classifications MeSH